Jove
Visualize
Contact Us

Related Concept Videos

Secondary Spinal Cord Injury llI: Pathophysiology01:25

Secondary Spinal Cord Injury llI: Pathophysiology

Early Ischemia and Ionic ImbalanceWithin minutes of spinal cord injury, a secondary cascade begins, progressing over hours to weeks. Vascular damage reduces blood flow, causing ischemia and mitochondrial dysfunction. ATP depletion leads to ion pump failure, membrane depolarization, sodium influx, potassium efflux, and water accumulation, resulting in cellular swelling. Increased intracellular calcium further disrupts mitochondria and accelerates cellular injury.Excitotoxicity and Neuronal...
Myasthenia Gravis ll: Pathophysiology01:22

Myasthenia Gravis ll: Pathophysiology

The disease process of myasthenia gravis begins at the neuromuscular junction, where antibodies attack key proteins needed for muscle activation. This immune reaction weakens signal transmission, leading to the characteristic muscle fatigue and weakness that define the condition.Immune-Mediated DamageIn most individuals, antibodies target acetylcholine receptors (AChRs) on the postsynaptic membrane of muscle cells. By blocking acetylcholine binding, these antibodies prevent the nerve signal...
Alterations in Muscle Tone lll01:11

Alterations in Muscle Tone lll

Rigidity and myotonia are distinct abnormalities of muscle tone that affect resistance and relaxation during movement. Although both involve altered muscle contraction, they arise from different neurological and muscular mechanisms.CharacteristicsRigidity is characterized by uniform resistance to passive movement across the entire range, independent of speed, affecting flexors and extensors equally. It may appear as lead-pipe rigidity (smooth, constant resistance) or cogwheel rigidity...
Cross-bridge Cycle01:26

Cross-bridge Cycle

As muscle contracts, the overlap between the thin and thick filaments increases, decreasing the length of the sarcomere—the contractile unit of the muscle—using energy in the form of ATP. At the molecular level, this is a cyclic, multistep process that involves binding and hydrolysis of ATP, and movement of actin by myosin.
Motor Units00:46

Motor Units

A motor unit consists of two main components: a single efferent motor neuron (i.e., a neuron that carries impulses away from the central nervous system) and all of the muscle fibers it innervates. The motor neuron may innervate multiple muscle fibers, which are single cells, but only one motor neuron innervates a single muscle fiber.
Multiple Sclerosis l: Introduction01:19

Multiple Sclerosis l: Introduction

Multiple sclerosis is a chronic autoimmune disease of the central nervous system (CNS) that affects the brain, spinal cord, and optic nerves. It is an inflammatory demyelinating disorder and a leading cause of neurological disability in young adults.EpidemiologyMS commonly begins between 20 and 40 years of age and is twice as common in women. Its exact cause remains unclear, but genetic susceptibility contributes, with higher risk in first-degree relatives and identical twins. A greater...

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Development of gene therapies-lessons from nusinersen.

Gene therapy·2017
Same author

Behavioral and electroantennogram responses of plum curculio, Conotrachelus nenuphar, to selected noxious plant extracts and insecticides.

Journal of insect science (Online)·2014
Same author

Phase II screening trial of lithium carbonate in amyotrophic lateral sclerosis: examining a more efficient trial design.

Neurology·2011
Same author

Mutant small heat shock protein B3 causes motor neuropathy: utility of a candidate gene approach.

Neurology·2010
Same author

The non-dystrophic myotonias: molecular pathogenesis, diagnosis and treatment.

Brain : a journal of neurology·2009
Same author

Inclusion body myositis: old and new concepts.

Journal of neurology, neurosurgery, and psychiatry·2009
Same journal

Medication Usage in Motor Neuron Disease and Spinal Muscular Atrophy: Insights from the Muscular Dystrophy Association Neuromuscular Observational Research Data Hub.

Journal of clinical neuromuscular disease·2026
Same journal

Severe Necrotizing Myositis With Anti-HMGCR and Anti-MDA5 Antibodies Without Cutaneous Involvement.

Journal of clinical neuromuscular disease·2026
Same journal

Diagnostic Nerve Ultrasound of Lateral Femoral Cutaneous Mononeuropathy With Focal Neural and Fascicular Enlargement.

Journal of clinical neuromuscular disease·2026
Same journal

Letter to the Editor: Utility of Smartwatches in Neuromuscular Disease: Current Use and Barriers to Adoption.

Journal of clinical neuromuscular disease·2026
Same journal

When Variants Collide: Mixed Clinical Presentation of Pharyngeal-Cervical-Brachial and Acute Motor Axonal Neuropathy Features in Guillain-Barré Syndrome.

Journal of clinical neuromuscular disease·2026
Same journal

Acute Motor Axonal Neuropathy in Biotinidase Deficiency Complicated by Dietary Restriction.

Journal of clinical neuromuscular disease·2026
See all related articles
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Experiment Video

Updated: Jun 27, 2026

ALS - Motor Neuron Disease: Mechanism and Development of New Therapies
15:48

ALS - Motor Neuron Disease: Mechanism and Development of New Therapies

Published on: July 29, 2007

Post-radiation lower motor neuron syndrome.

R W van der Sluis1, G I Wolfe, S P Nations

  • 1From the *Department of Neurology, University of Texas Southwestern Medical Center, Dallas, Texas, and the daggerDepartment of Neurology, Ohio State University School of Medicine, Columbus, Ohio.

Journal of Clinical Neuromuscular Disease
|December 17, 2008
PubMed
Summary
This summary is machine-generated.

Post-radiation lower motor neuron syndrome (PRLMNS) presents with weakness and muscle atrophy in areas exposed to radiation. This condition has a more favorable prognosis than amyotrophic lateral sclerosis.

More Related Videos

Paradigms of Lower Extremity Electrical Stimulation Training After Spinal Cord Injury
08:07

Paradigms of Lower Extremity Electrical Stimulation Training After Spinal Cord Injury

Published on: February 1, 2018

Standing Neurophysiological Assessment of Lower Extremity Muscles Post-Stroke
08:23

Standing Neurophysiological Assessment of Lower Extremity Muscles Post-Stroke

Published on: July 26, 2021

Related Experiment Videos

Last Updated: Jun 27, 2026

ALS - Motor Neuron Disease: Mechanism and Development of New Therapies
15:48

ALS - Motor Neuron Disease: Mechanism and Development of New Therapies

Published on: July 29, 2007

Paradigms of Lower Extremity Electrical Stimulation Training After Spinal Cord Injury
08:07

Paradigms of Lower Extremity Electrical Stimulation Training After Spinal Cord Injury

Published on: February 1, 2018

Standing Neurophysiological Assessment of Lower Extremity Muscles Post-Stroke
08:23

Standing Neurophysiological Assessment of Lower Extremity Muscles Post-Stroke

Published on: July 26, 2021

Area of Science:

  • Neurology
  • Oncology
  • Radiology

Background:

  • Post-radiation lower motor neuron syndrome (PRLMNS) is a known complication of radiation therapy for malignancies.
  • Descriptions of PRLMNS date back to World War II.

Purpose of the Study:

  • To describe the clinical features of four patients with PRLMNS.
  • To review the existing literature on PRLMNS.

Main Methods:

  • Evaluation of four patients who developed lower motor neuron syndrome after radiation therapy.
  • Description of clinical and electrophysiological features.

Main Results:

  • Patients exhibited weakness, atrophy, and fasciculations in radiation-exposed areas, with a mean onset of 14 years post-radiation.
  • Electromyography revealed denervation changes; MRI and myelography were unremarkable.
  • The condition showed a stable to slowly progressive course over a mean follow-up of 6.5 years.

Conclusions:

  • Clinicians should inquire about prior radiation exposure in patients with lower motor neuron syndromes.
  • PRLMNS offers a relatively favorable prognosis compared to amyotrophic lateral sclerosis.